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rs137854564

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137854564(C;C)
Make rs137854564(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position31235630
GeneNF1
is asnp
is mentioned by
dbSNPrs137854564
ebirs137854564
HLIrs137854564
Exacrs137854564
Varsomers137854564
Maprs137854564
PheGenIrs137854564
hapmaprs137854564
1000 genomesrs137854564
hgdprs137854564
ensemblrs137854564
gopubmedrs137854564
geneviewrs137854564
scholarrs137854564
googlers137854564
pharmgkbrs137854564
gwascentralrs137854564
openSNPrs137854564
23andMers137854564
23andMe allrs137854564
SNP Nexus

SNPshotrs137854564
SNPdbers137854564
MSV3drs137854564
GWAS Ctlgrs137854564
Max Magnitude0
OMIM613113
Desc
Variant0041
Relatedalso
ClinVar
Risk rs137854564(C;C)
Alt rs137854564(C;C)
Reference rs137854564(T;T)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29562648T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000000402.3,